用于确定抗病毒流感缺陷干扰颗粒优先级的基因组特征元分析。

IF 2.8 Q1 GENETICS & HEREDITY
NAR Genomics and Bioinformatics Pub Date : 2025-04-04 eCollection Date: 2025-06-01 DOI:10.1093/nargab/lqaf031
Jens J G Lohmann, Mia Le, Fadi G Alnaji, Olga Zolotareva, Jan Baumbach, Tanja Laske
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引用次数: 0

摘要

缺陷干扰颗粒(DIPs)是一种病毒缺失突变体,能阻碍病毒复制,因此是一种有效的新型抗病毒药物。为了评估可能的抗病毒疗法,我们首先需要深入了解 DIP 的特征。因此,我们对已发表的 20 个甲型和乙型流感病毒(IAV 和 IBV)体内和体外实验测序数据集进行了荟萃分析。我们分析了每个数据集的特征,如含缺失病毒基因组(DelVG)长度分布、直接重复和缺失位点的核苷酸富集。我们的分析表明,IAV 和 IBV 病毒序列在缺失时保留的 3'- 端和 5'- 端长度存在差异。此外,体外的 DelVG 往往比体内的短,这是一个新发现,对未来的 DIP 治疗设计具有潜在影响。此外,我们的分析表明,存在比预期序列更长的 DelVG,这可能与 DelVG 的另一种形成机制有关。最后,对来自 7 A/Puerto Rico/8/1934 数据集的 DelVGs 进行联合排序,发现了 11 个高度丰富但未被注意的候选者。总之,我们的研究强调了荟萃分析在发现未知的 DelVG 特性和预选候选抗病毒治疗设计方面的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Meta-analysis of genomic characteristics for antiviral influenza defective interfering particle prioritization.

Defective interfering particles (DIPs) are viral deletion mutants that hamper virus replication and are, thus, potent novel antiviral agents. To evaluate possible antiviral treatments, we first need to get a deeper understanding of DIP characteristics. Thus, we performed a meta-analysis of 20 already published sequencing datasets of influenza A and B viruses (IAV and IBV) from in vivo and in vitro experiments. We analyzed each dataset for characteristics, such as deletion-containing viral genome (DelVG) length distributions, direct repeats, and nucleotide enrichment at the deletion site. Our analysis suggests differences in the length of the 3'- and 5'-end retained in IAV and IBV viral sequences upon deletion. Moreover, in vitro DelVGs tend to be shorter than those in vivo, which is a novel finding with potential implications for future DIP treatment design. Additionally, our analysis demonstrates the presence of DelVGs with longer than expected sequences, possibly related to an alternative mechanism of DelVG formation. Finally, a joint ranking of DelVGs originating from 7 A/Puerto Rico/8/1934 datasets revealed 11 highly abundant, yet unnoticed, candidates. Together, our study highlights the importance of meta-analyses to uncover yet unknown DelVG characteristics and to pre-select candidates for antiviral treatment design.

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来源期刊
CiteScore
8.00
自引率
2.20%
发文量
95
审稿时长
15 weeks
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